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  4. NDC Product Code: 63135-924 Lubricaine 5

NDC 63135-924 Lubricaine 5

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63135-924?
  4. Lubricaine 5 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63135-924
Proprietary Name:
Lubricaine 5
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Esba Laboratories Inc.
Labeler Code:
63135
Product Label ID:
9d98afbf-11ce-745b-e053-2a95a90abc14
Start Marketing Date: [9]
03-20-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 63135-924?

The NDC code 63135-924 is assigned by the FDA to the product Lubricaine 5 which is product labeled by Esba Laboratories Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63135-924-04 113 g in 1 tube . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Lubricaine 5?

Cleanse affected area with mild soap and water. Gently dry by patting or blotting with toilet tissue or a soft cloth before application.Apply externally to the affected area up to 6 times daily.

Which are Lubricaine 5 UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Lubricaine 5 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".